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FLEXIBLE BIOPSY FORCEP

K871809 Class II Traditional
Decision Date
1987-06-18
Sponsor / Applicant
Surgi-Aid Endoscopics, Inc.

Technical Specification

510(k) Submission ID K871809
Product Code OCZ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1987-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLEXIBLE BIOPSY FORCEP received FDA 510(k) clearance under submission number K871809, sponsored by Surgi-Aid Endoscopics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1987-06-18.

Classification & Regulation

This clearance is catalogued under FDA product code OCZ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.